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Review
. 2020 Apr;104(4):675-681.
doi: 10.1097/TP.0000000000003024.

A Strategy for Suppressing Macrophage-mediated Rejection in Xenotransplantation

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Review

A Strategy for Suppressing Macrophage-mediated Rejection in Xenotransplantation

Akira Maeda et al. Transplantation. 2020 Apr.

Abstract

Although xenografts are one of the most attractive strategies for overcoming the shortage of organ donors, cellular rejection by macrophages is a substantial impediment to this procedure. It is well known that macrophages mediate robust immune responses in xenografts. Macrophages also express various inhibitory receptors that regulate their immunological function. Recent studies have shown that the overexpression of inhibitory ligands on porcine target cells results in the phosphorylation of tyrosine residues on intracellular immunoreceptor tyrosine-based inhibitory motifs on macrophages, leading to the suppression of xenogenic rejection by macrophages. It has also been reported that myeloid-derived suppressor cells, a heterogeneous population of immature myeloid cells, suppress not only NK and cytotoxic T lymphocyte cytotoxicity but also macrophage-mediated cytotoxicity. This review is focused on the recent findings regarding strategies for inhibiting xenogenic rejection by macrophages.

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References

    1. Bach FH. Xenotransplantation: problems and prospects.Annu Rev Med199849301–310
    1. Wennberg L, Rafael E, Liu J, et al. Allogeneic and xenogeneic islets are rejected by different and specific mechanisms: a study in rodents using a mixed allogeneic-xenogeneic islet transplantation model.Xenotransplantation19974228–234
    1. Lin Y, Vandeputte M, Waer M. Natural killer cell- and macrophage-mediated rejection of concordant xenografts in the absence of T and B cell responses.J Immunol19971585658–5667
    1. Fox A, Mountford J, Braakhuis A, et al. Innate and adaptive immune responses to nonvascular xenografts: evidence that macrophages are direct effectors of xenograft rejection.J Immunol20011662133–2140
    1. Yi S, Hawthorne WJ, Lehnert AM, et al. T cell-activated macrophages are capable of both recognition and rejection of pancreatic islet xenografts.J Immunol20031702750–2758

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